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  • Home
  • Global Regulatory Affairs Services
    • Introduction
    • Pharmaceutical
      • Requirements of Health Authorities
      • Drug Application Process
      • Meeting with Health Authorities
      • Electronic Common Technical Document (eCTD)
      • Register of Innovative Drugs
      • Submissions Comparing to Innovative Drugs
      • Product Monograph
      • Drug Label Compliance
      • Filing of Information and Material to Health Authorities
      • Evaluation of Submissions
      • Pharmacovigilance
    • Natural Health Products
      • NHP Documentation Review
      • NHP Product Registration Submissions
      • Natural Health Product Site Licence
    • Medical Device
      • Medical Devices Services
      • Medical Device Application Process
      • Medical Device class II, III and IV
  • Market Expansion Services
  • Contact Us
Atinza Canada Inc.Atinza Canada Inc.
  • Home
  • Global Regulatory Affairs Services
    • Introduction
    • Pharmaceutical
      • Requirements of Health Authorities
      • Drug Application Process
      • Meeting with Health Authorities
      • Electronic Common Technical Document (eCTD)
      • Register of Innovative Drugs
      • Submissions Comparing to Innovative Drugs
      • Product Monograph
      • Drug Label Compliance
      • Filing of Information and Material to Health Authorities
      • Evaluation of Submissions
      • Pharmacovigilance
    • Natural Health Products
      • NHP Documentation Review
      • NHP Product Registration Submissions
      • Natural Health Product Site Licence
    • Medical Device
      • Medical Devices Services
      • Medical Device Application Process
      • Medical Device class II, III and IV
  • Market Expansion Services
  • Contact Us

ATINZA CANADA INC. Global Expertise in Regulatory Affairs Get the growth you need to succeed Market Expansion Services RESPONSIBLE & RELIABLE We value our prestige with customers Caption Text4 We stand by our commitment Better - Faster - Easier No compromise over Quality Passion for excellence

Global Regulatory Affairs Services

  • Provides regulatory assessment, strategy, and guidance for the clients to customize to theirs unique needs and budgets
  • Work closely with clients to ensure label of pharmaceutical products will comply strictly with the labeling requirements
  • Provide ongoing submission expertise to achieve regulatory approval
    Advise clients relating requirements in other relevant regulatory guidelines, policies and technical documents.

Market Expansion Services

  • Coordinating market research
  • Planning, developing and organizing marketing activities to support sales objectives
  • Create promotional strategies and campaigns to reach target sale quantities.
  • Advising on selection of products, pricing, advertising and sales promotion, selling, and distribution channels according to market demands.

Trading partner

  • Provide sourcing solution for customers for all products they need. We find trust worthy partners/manufacturers will can provide long term flow of products and ensure shipment are handled timely and smoothly.
  • Ensure strict supply standards and only establish business relationship with  ethical suppliers. Our commitment is to assure win-win for both customers and suppliers and mutual and sustainable development for both parties.

Contact Us

Please let us know if you have any inquiries.

Send Message

Atinza provides timely but yet effective regulatory affairs services for all stages of your products’ development and lifecycle management.

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Global Regulatory Affairs Services

Market Expansion Services

Contact Us

 

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Introduction

Pharmaceutical

Natural Health Products

Medical Device

 

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